|
Early onset or syndromic epilepsy v1.191
|
COG6
|
Rebecca Foulger Source Wessex and West Midlands GLH was added to COG6.
|
|
Early onset or syndromic epilepsy v1.190
|
COG6
|
Rebecca Foulger Source NHS GMS was added to COG6.
|
|
Early onset or syndromic epilepsy v1.189
|
COG6
|
Rebecca Foulger reviewed gene: COG6: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
|
|
Early onset or syndromic epilepsy v1.188
|
COG6
|
Tracy Lester reviewed gene: COG6: Rating: AMBER; Mode of pathogenicity: ; Publications: 20605848; Phenotypes: Congenital disorder of glycosylation type IIl, 614576 , Shaheen syndrome, 615328; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
|
|
Early onset or syndromic epilepsy v0.1589
|
COG6
|
Sarah Leigh Marked gene: COG6 as ready
|
|
Early onset or syndromic epilepsy v0.1589
|
COG6
|
Sarah Leigh Added comment: Comment when marking as ready: Based on reviewers' comments.
|
|
Early onset or syndromic epilepsy v0.1589
|
COG6
|
Sarah Leigh Gene: cog6 has been classified as Amber List (Moderate Evidence).
|
|
Early onset or syndromic epilepsy v0.1589
|
COG6
|
Sarah Leigh Publications for gene: COG6 were set to
|
|
Early onset or syndromic epilepsy v0.1440
|
COG6
|
Sarah Leigh Mode of inheritance for gene: COG6 was changed from to BIALLELIC, autosomal or pseudoautosomal
|
|
Early onset or syndromic epilepsy v0.1439
|
COG6
|
Sarah Leigh Added comment: Comment on phenotypes: Congenital disorder of glycosylation, type Iil 614576
|
|
Early onset or syndromic epilepsy v0.1439
|
COG6
|
Sarah Leigh Phenotypes for gene: COG6 were changed from to Congenital disorder of glycosylation, type Iil 614576
|
|
Early onset or syndromic epilepsy
|
COG6
|
Zornitza Stark reviewed gene: COG6
|
|
Early onset or syndromic epilepsy
|
COG6
|
Sarah Leigh Added gene to panel
|